ZMP
zfpm1
Ensembl ID:
ZFIN ID:
Description:
Zinc finger protein FOG1 [Source:UniProtKB/Swiss-Prot;Acc:P60622]
Human Orthologue:
ZFPM1
Human Description:
zinc finger protein, multitype 1 [Source:HGNC Symbol;Acc:19762]
Mouse Orthologue:
Zfpm1
Mouse Description:
zinc finger protein, multitype 1 Gene [Source:MGI Symbol;Acc:MGI:1095400]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10486 | Nonsense | Available for shipment | Available now |
sa36619 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36618 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10486
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060949 | Nonsense | 85 | 1191 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 16992143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17343909 |
GRCz11 | 18 | 17332975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGCARTGKCAGACGAGGGCGAKGAAGATGAGAAAGGACTGAAGCGCTG[C/A]AYAGAAGATGAAGAGGAGGAAGAKGTGGACAGGGAAGGGGAACCCCASTG
Long Flanking Sequence:
CGGCTAAATTTTCCGTAGTGTATGTGTGTGAATGAGTATGTGTGGATGTTTCCTAGAGATGGGTTGCAGCTGGAAGGGCATAAAGCGTAAAGCATATGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGTGACCCCGGATTAATAAAGGGACTAAGCCGAAAAGAAAATGAATGAATGTTGATGTACTTGGAATATTAAGTAGGAGGTGGGATCATTCAATCATAGCAAACTGTTAGAGGAGGCGTGGTTAAGACTGATGTGGCTGAAGTATTCCGCCACTCTAAATGCTGAGGCATCTGATCAGACTTTGATTGAAACAAACTTTTTTCCTCCACGGATTATTTGTTCACCGAACAAATAACACAATGTGCACTTGCAAAATAAACATTGTCAACCTTGACTTTTAATTTTTACTCTGGCTGTCCACAGAGCCAAGAACGCACGAGTCTCTGGCAATGGCAGACGAGGGCGAGGAAGATGAGAAAGGACTGAAGCGCTG[C/A]ACAGAAGATGAAGAGGAGGAAGAGGTGGACAGGGAAGGGGAACCCCAGTGGAACGGCCCAGGTCAGTCTCTATCTGTGTCTCCTTCAGGGGTGTTTAACTGAACCATGAGTCACTGGATTCTCAGGAAGGGCCAGTCGTAGTCATACTGTCAGCCGGGCGGCCACAAAACAATATAGGCCACGACTTTATCATGCTCCACACGCAAAACAGAAATGATCCAATCTGAGCTGCCTGTAAATTTGGAGAGTGTACTGTAAGTCATCAGTGGAGCTGGCCTTCTGTATGGCTCCCAACAATTAGTCACTTTTTCTGGTTCAACACAGTTCAGTGACATCACACTTGCATCACGTCTGAGAATTCAGCCAGTTCAGATAAACTTTCAAACGAGCCTCATTAAACATTGCTTTACCTCCAGGGTTAAATCAGAGAGTTATCATGACTGTTGACTCGAAAAATAGAAAACTTACTTTTATTGAACGCACAACATCTCTAATATTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36619
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060949 | Nonsense | 522 | 1191 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 16932620)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17284386 |
GRCz11 | 18 | 17273452 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAGAGGAGCCACGTTCAGACTATGAAAACGATGCAAAGGAAGAAGAA[C/T]AAGTGAACAGTCCTCAAGAAAATGCTGCAGAGGCAAGCTCATCTCAGCCT
Long Flanking Sequence:
TAGATGAGGGATTACTTCAAGTCCTCTCTCTTTCTCCTAAGCTGTATAAGAACTATTCATCAAACCTGATGACCTTTAAAATAGTTTAAACATAAGTGTTCTTGATCATAAGGTTTAAAGTCATCATTCTATATCTGAATGTCTGTCATTTTTTCCACTTTGTGACAGGCTTGAGTCCAGGAGACTCTGGCATTGTTCTGAAATGTCAGGTGTGCGGCTACTCTGCTGACACTCCTGCATTACTTCAGCAGCATGTCCACACACACCTGGAAGTGAGGGTTCCAGCTGAGAGGAGCCCCACACCTCGCCAGAGCAGTCCTCCTTCTTCTGAGCTCCCTGAGCTGCAAGAAACGGAGCCTGCTGCCTGCGTGCCCCGACCTGACTCGTCCAGCCCTGGAGCCAATGGCAGCTCAGCCTCTCAGGGCTACAGTCCCCTCAGCCAACTCAACATCAAAGAGGAGCCACGTTCAGACTATGAAAACGATGCAAAGGAAGAAGAA[C/T]AAGTGAACAGTCCTCAAGAAAATGCTGCAGAGGCAAGCTCATCTCAGCCTACTTCACCTAAGAGCCCCACCGTGGTTGCAGTGAAAGCAGAGCCGGCCAGTCCCACCCCAGGTTCTAGTCCTGCACATTCTGGAACAGGGGGTTCAGTTCTCCCTGGAGGAGCAGTGTTCTTGCCGCAGTACATGTTTAATTCTGAGGCGGCCATAATGCCCCAGGCATCTGAGATTCTGGCTAAGATGTCTGAGATGGTGCACAGTAGACTTAAACAGGGACAAGGACCAGCAGCTGCACAGCAGAGCTTCTACCCACCAGGCTCTCCTGCCAGCGTTCACAAGGGAGCTACCTGCTTCGAATGTGACATTACCTTCAACAACATTAACAACTTCTATGTCCACAAGAGGCTTTACTGCTCCAGCAGGCATCAACAAGGAGAGACTGGAGGCCTTGTGAAGGAAGGGGCTGTTACTGCAGCTGCTCCTCCTGTTTCCCACGCTGCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36618
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060949 | Nonsense | 812 | 1191 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 16931750)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17283516 |
GRCz11 | 18 | 17272582 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATCCCACCAACCAGCGCCCCCATTCTGGCAAGGCTGCCTTCCTACCC[C/T]AACCTATCCGCACACGCAAACGTAAGAAGATGTATGAGATCCACATGGCT
Long Flanking Sequence:
ACAACATTAACAACTTCTATGTCCACAAGAGGCTTTACTGCTCCAGCAGGCATCAACAAGGAGAGACTGGAGGCCTTGTGAAGGAAGGGGCTGTTACTGCAGCTGCTCCTCCTGTTTCCCACGCTGCTTCACCCCAGGCCAGACCAGTCAGCCGTGCAGCTTCAGCCTCTCCTAGCTGCCCTGACCCTGCACCAGGAGGAACGGCCTCGGAACCCAAGGTAGTGGAGGTGAAAATTGAGGATCCAGGGCTGAAAGATGCTACCTGCTCATCGTCCTCAGAGGGAGAGGGACCTGGGGGCGGGCAAGCCAGCGAAGGTAGCCAAAGTCCTAGTGGATCTGCTGAAGACCAAGATGACGACCCCACTCGCACATTTTGCCAGGCATGCAACATTCGCTTCAGCCGTCATGACAACTACATTGTCCACAAGCGATTCTACTGCGCCTCTAGACATGATCCCACCAACCAGCGCCCCCATTCTGGCAAGGCTGCCTTCCTACCC[C/T]AACCTATCCGCACACGCAAACGTAAGAAGATGTATGAGATCCACATGGCTCAAACTGAGGCTTTGGCTAATGCCACTACTTTGCCAGCAGGAACTAGTTTGGGGGTTAACCAAGAGGGCTCTTCCGTTGCTCTATTGTCCCAAGTGTCAACTCCTACACGCAGCTCAAGTCCTGAAGGAGAAGGACCCATAGACTTGAGTAAAAGACCCAGACTAAGAGAGAGCCAGAGAAAGGACAGCATTTCTGCATTGCCCCTTTCTGACTACCACAAGTGCACTGCTTGCAGCATTAGCTTCAACAGTATTGAGAACTACTTGGCCCACAAGACCTACTACTGCCCAGCCACTACCCTGCAACCACAAACTATGGAGCAACTAAACCGACTGAAGAGGCCTACCTCCACCTCACCGAAGAACAGAGCCGTGGACCAGCACTCTGATTCCAAAGTGCTTCAAACAGGTAAAACCGCAGCTGTTGCACATGCTGTACCTGGCTCAGAG
Associated Phenotype:
Not determined